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US: Sr. Clinical Research Associate

Date: 15-Aug-2014
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US - Sr. Clinical Research Associate

∑ Assists with, attends, and may present at Investigator Meetings for assigned studies.

∑ Performs study close-out visits.

∑ Serves as mentor for more junior CRAs as well as new CRAs to the project.

∑ May conduct field training and assessment of CRA Is and CRA IIs.

∑ Authorized to request site audits for reasons of validity.

∑ Performs other duties as requested.

∑ Strong knowledge of clinical research process and medical terminology.

∑ At least four years experience in monitoring clinical trials preferred.

∑ Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.

∑ Excellent organizational and interpersonal skills.

∑ Ability to interact with all levels of staff to coordinate/execute study activities.

∑ Ability to handle several priorities within multiple, complex clinical trials.

∑ Ability to reason independently and recommend specific solutions in clinical settings.

∑ Able to mentor other CRAs on project team and co-monitor as required.

∑ Understanding of basic data processing functions, including electronic data capture.

∑ Understanding of current GCP/ICH guidelines applicable to the conduct of clinical research.

∑ Able to qualify for a major credit card.

∑ Valid driverís license; ability to rent automobile.

∑ Willingness and ability to travel domestically and internationally, as required.

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